M16K (p.Met16Lys) variant of PIK3CA (P42336)
M16K (p.Met16Lys) in PIK3CA (P42336) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
M16K (p.Met16Lys) variant details
- p.Met16Lys
- Ensembl rs2108385129
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available